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Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126

Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126

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Page 1: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126

Evaluating cell lines as tumor models by comparison

of genomic profiles

Domcke, S. et al. Nat. Commun 4:2126

Page 2: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126

MotivationProblem: Genomic differences between

cancer cell lines and tissue samples

TCGA and CCLE provide molecular profiles for tumor samples and cell lines

Compared high-grade serous ovarian cancer (HGSOC) to genomic profiles to identify suitable cell lines for in vitro models

Page 3: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126

Ovarian Cancer

Over 100,000 women die of ovarian cancer each year

5th leading cause of cancer deathDivided into 4 major histological subtypes:

Serous (study’s focus)EndometrioidClear CellMucinous carcinoma

Page 4: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126

Common cell line models for ovarian cancer and HGSOC are: SK-OV-3, A2780, OVCAR-3, CAOV3 and IGROV1

Need for well-characterized cell line models for cell types

Found differences between most common models and majority of HGSOC samples

Page 5: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126
Page 6: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126

Analyzed 316 HGSOC tumor samples from TCGA and 47 ovarian cancer cell lines from CCLE

DNA copy-number, mutation and mRNA expression data Fraction genome altered (FGA):

CN=log2(sample intensity/reference intensity)

L(i) is length of segment i

T is threshold value of Cni above which segments are altered

- T= 0.2 for TCGA samples- T=0.3 for CCLE cell lines

Page 7: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126
Page 8: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126
Page 9: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126

Suitability of HGSOC Models

S = A + B – 2×C – D/7

A = Correlation with mean CNA of tumorsB = 1 for cell lines with TP53 mutation or else 0C = 1 for hypermutated cell line or else 0D = # of genes mutated in 7 “non-HGSOC” genes

Page 10: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126
Page 11: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126
Page 12: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126
Page 13: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126
Page 14: Evaluating cell lines as tumor models by comparison of genomic profiles Domcke, S. et al. Nat. Commun 4:2126

Future Directions

• Drug response profiles using accurate cell line models with known alterations for patient selection in clinical trials

• Perform preclinical drug screens for more-informed patient therapy

• Any others?